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B Wermuth

Showing results (51-60 of 87) with videos related to

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Journal of Inherited Metabolic Disease|January 14, 1998
N-Acetylglutamate synthetase deficiency responding to carbamylglutamateJ Hinnie, J P Colombo, B Wermuth, et al.
Biochimica Et Biophysica Acta|February 9, 1979
Amidination of amino groups of aldehyde reductase from human liverB Wermuth, J D Münch, J Hajdu, et al.
Human Mutation|January 1, 1997
Ornithine transcarbamylase deficiency: ten new mutations and high proportion of de novo mutations in heterozygous femalesE Oppliger Leibundgut, S Liechti-Gallati, J P Colombo, et al.
The American Journal of Clinical Nutrition|September 30, 2000
Antioxidant and thyroid hormone status in selenium-deficient phenylketonuric and hyperphenylalaninemic patientsM M van Bakel, G Printzen, B Wermuth, et al.
Clinical Genetics|March 22, 2001
Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codonE Ploechl, W Ploechl, S Stoeckler-Ipsiroglu, et al.
Alcoholism, Clinical and Experimental Research|December 1, 1988
Degradation of aliphatic alcohols by human liver alcohol dehydrogenase: effect of ethanol and pharmacokinetic implicationsT Ehrig, K M Bohren, B Wermuth, et al.
Human Genetics|February 1, 1996
Identification of four novel splice site mutations in the ornithine transcarbamylase geneE Oppliger Leibundgut, B Wermuth, J P Colombo, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcomeC Bannwart, B Wermuth, R Baumgartner, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activityM Staudt, B Wermuth, P Freisinger, et al.
Hepatology (Baltimore, Md.)|December 1, 1996
A novel two-nucleotide deletion in the ornithine transcarbamylase gene causing fatal hyperammonia in early pregnancyU Schimanski, D Krieger, M Horn, et al.
Pageof 9

Showing results (51-60 of 87) with videos related to

Sort By:
Pageof 9
Journal of Inherited Metabolic Disease|January 14, 1998
N-Acetylglutamate synthetase deficiency responding to carbamylglutamateJ Hinnie, J P Colombo, B Wermuth, et al.
Biochimica Et Biophysica Acta|February 9, 1979
Amidination of amino groups of aldehyde reductase from human liverB Wermuth, J D Münch, J Hajdu, et al.
Human Mutation|January 1, 1997
Ornithine transcarbamylase deficiency: ten new mutations and high proportion of de novo mutations in heterozygous femalesE Oppliger Leibundgut, S Liechti-Gallati, J P Colombo, et al.
The American Journal of Clinical Nutrition|September 30, 2000
Antioxidant and thyroid hormone status in selenium-deficient phenylketonuric and hyperphenylalaninemic patientsM M van Bakel, G Printzen, B Wermuth, et al.
Clinical Genetics|March 22, 2001
Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codonE Ploechl, W Ploechl, S Stoeckler-Ipsiroglu, et al.
Alcoholism, Clinical and Experimental Research|December 1, 1988
Degradation of aliphatic alcohols by human liver alcohol dehydrogenase: effect of ethanol and pharmacokinetic implicationsT Ehrig, K M Bohren, B Wermuth, et al.
Human Genetics|February 1, 1996
Identification of four novel splice site mutations in the ornithine transcarbamylase geneE Oppliger Leibundgut, B Wermuth, J P Colombo, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcomeC Bannwart, B Wermuth, R Baumgartner, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activityM Staudt, B Wermuth, P Freisinger, et al.
Hepatology (Baltimore, Md.)|December 1, 1996
A novel two-nucleotide deletion in the ornithine transcarbamylase gene causing fatal hyperammonia in early pregnancyU Schimanski, D Krieger, M Horn, et al.
Pageof 9